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Updated: May 20, 2026

Preparation Of Neovascular Tissues from Human Glioma Tissues for Quantitative Proteomics Analysis of Tumor Angiogenesis
Published on: March 20, 2026
Antiangiogenic therapy in the management of brain tumors: a clinical overview
Saroj Kunnakkat1, Maya Mathew, Ashwatha Narayana
1Department of Radiation Oncology, New York University Langone Medical Center, NY 10016, USA. ashwatha.narayana@nyumc.org
Abstract:
Central to the process of brain tumor development is angiogenesis, which involves a host of molecules and receptors. In recent years, antiangiogenic therapies have been developed and tested for their effectiveness against these tumors. Among them are inhibitors against vascular endothelial growth factor and its receptors, as well as inhibitors targeting the platelet-derived growth factor family, integrins, and histone deacetylase. While many have been shown to be effective with limited toxicity, some tumors are able to adopt escape mechanisms. Further research is needed in the development of effective multi-targeted agents to reduce these effects.
Insights
Antiangiogenic therapies targeting brain tumor growth show promise but face resistance. Developing multi-targeted agents is crucial to overcome tumor escape mechanisms and improve treatment effectiveness.
Area of Science:
- Neuro-oncology
- Cancer Biology
- Molecular Medicine
Background:
- Angiogenesis is critical for brain tumor development, involving numerous molecular targets.
- Antiangiogenic therapies have emerged as a treatment strategy for brain tumors.
- Current therapies include inhibitors of vascular endothelial growth factor, platelet-derived growth factor, integrins, and histone deacetylase.
Purpose of the Study:
- To review the development and effectiveness of antiangiogenic therapies for brain tumors.
- To discuss the challenges posed by tumor escape mechanisms.
- To highlight the need for novel therapeutic strategies.
Main Methods:
- Literature review of antiangiogenic agents and their mechanisms of action.
- Analysis of clinical trial data on the efficacy and toxicity of these therapies.
- Examination of known tumor resistance pathways.
Main Results:
- Several antiangiogenic agents demonstrate efficacy with manageable toxicity.
- Tumors can develop resistance through various escape mechanisms.
- Combination therapies and multi-targeted agents show potential in preclinical studies.
Conclusions:
- Antiangiogenic therapies are a valuable addition to brain tumor treatment.
- Overcoming therapeutic resistance is a key challenge.
- Further research into multi-targeted agents is essential for improved patient outcomes.
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